phendimetrazine tartrate
- Product NDC
- 71335-0110
- 11-digit product format
- 713350110
- Labeler code
- 71335
- Product ID
- 71335-0110_98aeb7de-8659-4e65-9f37-c0dce28e63b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- phendimetrazine tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA089452
- Marketing category
- ANDA
- Marketing start
- 2000-04-06
- Marketing end
- 0000-00-00
- Substance
- PHENDIMETRAZINE TARTRATE
- Active strength
- 35 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record